CTNNB1 综合征认知和行为症状的系统回顾。

IF 5.4 2区 心理学 Q1 NEUROSCIENCES
Mercè Pallarès-Sastre, Imanol Amayra, Monika Salgueiro, Elena Villanueva-Viar, Amaia Lasa-Aranzasti, Maitane García
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引用次数: 0

摘要

CTNNB1综合征是一种罕见的神经发育障碍,由CTNNB1基因的可能致病性或致病性变异引起。我们进行了一项系统的回顾,以检查先前提供CTNNB1综合征患者的研究,特别是那些描述智商、运动发育、语言障碍、行为问题和自闭症特征的研究。研究的数据库是PubMed和Scopus。纳入标准为(a)经基因检测确诊为CTNNB1综合征的报告人类患者;(b)与认知、智商、运动发育、语言障碍、行为问题或自闭症特征有关;(c)没有其他基因诊断(d)用西班牙语或英语书写。共纳入42项研究。总的来说,所描述的症状非常不均匀,患者的损害程度不同。然而,个体达到最重要的发展里程碑比预期晚,并有不同程度的损害。在大多数研究中,很少使用标准化方法来评估认知和行为领域,而且绝大多数研究不包括基于CTNNB1综合征个体症状的特定评估方案。此外,只有两名成年患者进行了深入的描述,这意味着该综合征在以后的生活中还有许多未知的进展。因此,未来的研究应侧重于通过标准化方案增加评估的样本和计数,以表征CTNNB1综合征的认知和行为表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Systematic Review of Cognitive and Behavioural Symptoms in CTNNB1 Syndrome.

CTNNB1 syndrome is a rare neurodevelopmental disorder caused by a likely pathogenic or pathogenic variant in the CTNNB1 gene. A systematic review was conducted to examine previous research that provided CTNNB1 syndrome patients, specifically those that described intellectual quotient, motor development, language impairments, behavioural problems and features of autism. Databases examined were PubMed and Scopus. The inclusion criteria were (a) reported human patients diagnosed with CTNNB1 syndrome by a genetic test; (b) were related to cognition, intelligence quotient, motor development, language impairment, behavioural problems or features of autism; (c) did not have another genetic diagnosis and (d) were written in Spanish or English. A total of 42 studies were included. Overall, the symptomatology described was very heterogeneous with varying degrees of impairment among patients. However, individuals reached most significant developmental milestones later than expected and with different degrees of impairment. The use of standardised methodology to assess cognitive and behavioural domains was scarce in most studies, and the vast majority did not include a specific assessment protocol based on the symptomatology of CTNNB1 syndrome individuals. In addition, only two adult patients were described in depth, which implies that there are many unknowns about the progression of the syndrome later in life. Therefore, future research should focus on increasing the sample assessed and count with a standardised protocol in order to characterise the cognitive and behavioural phenotype of CTNNB1 syndrome.

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来源期刊
Neuropsychology Review
Neuropsychology Review 医学-神经科学
CiteScore
11.00
自引率
1.70%
发文量
36
期刊介绍: Neuropsychology Review is a quarterly, refereed publication devoted to integrative review papers on substantive content areas in neuropsychology, with particular focus on populations with endogenous or acquired conditions affecting brain and function and on translational research providing a mechanistic understanding of clinical problems. Publication of new data is not the purview of the journal. Articles are written by international specialists in the field, discussing such complex issues as distinctive functional features of central nervous system disease and injury; challenges in early diagnosis; the impact of genes and environment on function; risk factors for functional impairment; treatment efficacy of neuropsychological rehabilitation; the role of neuroimaging, neuroelectrophysiology, and other neurometric modalities in explicating function; clinical trial design; neuropsychological function and its substrates characteristic of normal development and aging; and neuropsychological dysfunction and its substrates in neurological, psychiatric, and medical conditions. The journal''s broad perspective is supported by an outstanding, multidisciplinary editorial review board guided by the aim to provide students and professionals, clinicians and researchers with scholarly articles that critically and objectively summarize and synthesize the strengths and weaknesses in the literature and propose novel hypotheses, methods of analysis, and links to other fields.
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